Msi 769-60

by Modern Surgical Instruments LLC

Msi 769-60 is a Class I device made by Modern Surgical Instruments LLC, listed in FDA GUDID since 18 Jan 2023 (UDI-DI 00810130200184), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00810130200184 UDI-DI	Date18 Jan 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00810130200184

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Msi
Generic name: Surgical retractor/retraction system blade, reusable
Model / reference: 769-60

Primary DI / UDI-DI: 00810130200184
FDA product code: GAD
GMDN term: Surgical retractor/retraction system blade, reusable

Device class: Class I
Regulation number: 878.4800
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number

Other properties (11, all answered No)